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1. Diagnostic concerns in fluency disorders
2. Fluency Assessment
3. Assessment Overview
4. The goals of a fluency evaluation For young children:
Do they stutter?
Developmental stuttering vs. normal disfluency vs. language formulation disfluency
If they stutter, how likely is recovery? – examination of risk factors
What is the appropriate next step?
Monitoring, parental consultation
Indirect management
Direct management
For older children and adults:
How significant is the stuttering problem?
In terms of overt symptoms
In terms of associated behaviors, including frustration, fear, avoidance, and perceptions of handicap and disability
What factors affect fluency and associated affective and emotional states?
What are the goals of fluency therapy?
5. Appraising overt symptoms: the speech sample From children:
Conversation with you and with the parents
Narrative (e.g., “Frog” stories)
Recreation of situations/contexts in which fluency is reported to wax and wane
From adults:
Monologue (may be done during case history)
Conversational interaction
Reading
Optional: appraise consistency and adaptation using repeated reading of materials
6. Tallying disfluencies (overt behaviors) from the speech sample What gets counted?
Normal disfluencies
Stutter-like disfluencies (SLDs)
Calculating proportions – what are your numerators and denominators?
Appraising frequency
Via percent stuttered words or syllables
Problems with purely time-based measures
Describing typology
What are the proportional incidences of major disfluency subtypes?
Reliability of behavioral measurements – Tom exercise
7. Examining accessory features A tip: listen to the tape without looking, then look without listening
Things to look for:
Atypical speech production postures
Ancillary body movements
Eye gaze
Sample assessment instruments: SSI-3, Cooper Scales
8. Attitude assessment Potential measures:
See sample handouts How does stuttering affect the individual’s everyday behavior?
What are perceptions of disability and handicap?
How do they feel about speaking and stuttering?
What do they know or believe about their stuttering?
9. Goals of the assessment For parents, what are the goals? Can they supply more than one?
Using goals to explore options
What are the client’s goals?
10. Dx summary – preschool children Questions that need to be answered:
Is it stuttering?
What is the likelihood of spontaneous recovery?
What has been done up to now, with what results?
What are the pro’s and con’s of various treatment models?
11. Preschoolers (continued) Information required:
Frequency, duration and types of disfluency
Presence of struggle or tension
Presence of awareness and reactions to moments of disfluency
Assessment scales (see handouts)
Status of other speech/language abilities
Parent-child communicative style
Parents’ reactions and attitudes toward behaviors
Parents’ understanding of the nature of stuttering
Perceived risk factors for chronicity or worsening of symptoms
12. Preschoolers (continued) Case history specifics:
Parents’ information about onset, course of disfluency patterns over time
Medical, social and developmental history
Child and listener responses to disfluency
Level of awareness, frustration, avoidance, self-consciousness
Reactions of others in the child’s environment, including advisements
Parents’ beliefs about cause of the problem
Parents’ views of the child’s personality and temperament
Family history of stuttering and other communicative disorders
13. Behavioral measures for pre-schoolers: What are SLDs? Stutter-like disfluencies include:
Sound, syllable and monosyllabic whole word repetitions
Weighted scores for disfluency take into account the number of iterations
Blocks, prolongations, broken words
Other disfluencies might include:
Interjections, filled pauses
Revisions
Multisyllabic word or phrase repetitions
Hesitations
14. Step Two: Assess predictors of remission and chronicity The facts:
~80% of children who begin to stutter will recover (apparently without clinical intervention)
The time frame for remission may be more limited than previously supposed (Yairi, et al., 1996; Ramig, 1993)
15. Predictors of chronicity and remission*
16. Weighing the odds
17. Patterns to monitor
18. “Watch and see”, not wait and see As in SLI, the rapid course of remission, but uncertain future of individual children requires the partnership of parents and clinician to actively monitor progress and establish guidelines for implementing intervention (Paul, 2000)
19. Dx summary: school-aged children Questions that need to be answered:
How complex has problem become? (awareness, shame, guilt, self-image as a CWS?)
Is any part of problem language-based?
What are relative contributions of physiological factors, psychological factors, attitudes and learning?
What is child’s perception of problem? How does it compare to the parents’ perceptions?
What intervention strategies would be most beneficial?
In what capacities will parents/school be involved?
Educational component
Coordination of services
20. School-aged children (continued) Information required:
Medical, developmental, social and educational history
Full understanding of speech/language abilities
Frequency, duration, concomitant behaviors
Impact on emotional development
Parental/family/school reactions and attitudes toward stuttering
Child and parents’ understanding of the nature of stuttering
Previous speech therapy: approaches and outcomes
Listener reactions and responses to listener reactions
23. School-aged children (continued) Parent interview: similar to that of preschoolers; adjust to be age-appropriate
Teacher interview
General questions about achievement and social development
How does stuttering affect these areas?
Reactions of students and staff to stuttering?
Child’s reaction?
Level of participation, verbally and nonverbally in classroom and other school activities
Information about services received at school
24. School-aged children (continued) Child interview
Move slowly until you assess how direct or open the child would like the interview to be
Child’s perception of the problem – what does he call it?
Child’s perception of parents’ perception of the problem
Child’s description of the problem
How much does stuttering bother the child?
What does the child do to cope with or escape from the moment of stuttering?
Experiences with peers: teasing, support?
Assessment scales (see handouts, e.g. CALMS model)
Attitude scales: CAT (DeNil & Brutten)
25. Tips for interviewing young children Some basics:
Don’t be alarmed if child says, “I don’t know” or shrugs shoulders. Children are not used to evaluating feelings. They don’t necessarily evade. Some children just accept things the way they are.
Share something about yourself, and the type of work you do:
“One of my jobs is to help kids talk better”
26. Talking to young children (continued) Use analogies and examples to help the child feel comfortable talking about problems.
For example, “One of my friends who comes to play with me is Josh. He sometimes gets stuck when the teacher asks him to read to the class. Does that ever happen to you?”
Use a marble maze with some marbles too large to flow freely. Have some get stuck. Then say, “This marble is s-s-s-stuck. That picture on the wall was made by Josh. It shows how he crunches up his face when he gets stuck. What kinds of things do you do?”
27. Some questions to ask young children Whom do you like to talk to? (At home, at school)
Who talks the most/least (At home, at school)
Who interrupts? Who do you interrupt?
Who are good talkers?
When do you want to talk well?
Are there times you want to talk extra well?
Do other people feel this way as well?
When do you want to talk more than you do?
Who listens/pays attention?
What do you like listeners to do when you talk to them?
28. Qualifying children for services in the schools Please see diagnostic considerations for qualifying CWS under IDEA and writing IEPs (separate handout).
29. Dx summary - Adults Questions you need to answer:
What type of fluency disorder is it?
Developmental stuttering
Cluttering
Neurogenic stuttering
Psychogenic stuttering
If developmental stuttering, what are the relative contributions of physiological, psychological, attitudinal factors and learning?
Why does the client seek tx now? – goals?
How does disfluency affect client’s communication and life?
What intervention strategies will be most appropriate?
30. Adults (continued) What information will be needed?
Disfluency types
Severity of the disorder
Percentage of disfluencies
Concomitant behaviors
Fears and avoidances
Client’s attitude toward disorder
Core and secondary behaviors
Emotional reactions/attitudes
Social, vocational and lifestyle information
31. Adults (continued) Interview specifics:
Onset and early development; how was stuttering handled in family? What does client believe caused it?
Impact educationally, socially and vocationally
Outlook: hope for change, past tx experiences, motivation to change
Patterns of recovery and relapse, situational variability
Family history
Level of fear of speaking and stuttering
Avoidance patterns
Self-perceptions
32. Adults (continued) Measuring impairment, disability and handicap (Yaruss & Quesal)
Speaker’s reaction to stuttering
Functional communication
Quality of life
33. Measuring speaker reactions: tools Watson (1998) Inventory of communication attitudes
Ornstein & Manning (1985) Self-Efficacy Scale (SEA-Scale) for Adults who Stutter
Andrews & Cutler (1974) – adaptation of Erickson’s S-Scale
Yaruss & Quesal (2000)
34. Diagnostic interpretation For children
Provide data on prognostic indicators, and work with parents to determine next steps, which should include a minimum of active monitoring and counseling to palliate symptoms.
Introduce information about therapy approaches
Provide information and information sources to help family explore stuttering.
35. For adults:
Explain the therapy approaches that you offer, and explore acceptability to client. Is this what the client had in mind?
Negotiate the “terms” of therapy
Help them become informed consumers; provide information sources.